It is not enough to enhance efficiency or accuracy; we must embed transparency, temporal awareness and systemic oversight ...

The University IRB applies all Department of Health and Human Services (DHHS) requirements for informed consent to greater than minimal risk research: DHHS general requirements (at 45 CFR 46.116) (see ...

Informed consent (IC) is a fundamental aspect of ethical clinical research, safeguarding the rights and well-being of participants. It empowers participants with comprehensive information about the ...

Obtaining informed consent is a basic ethical obligation and a legal requirement for researchers. This requirement is founded on the principle of respect for persons. Potential participants must be ...

The Forms and Templates page includes templates for informed consent documents.. However, because each human participants research (HSR) proposal is different and carries unique risks to participants, ...

Key features of informed consent include disclosure of all details about the trial—from how far a subject may need to travel to get to a research site to potential side effects—as well as ...